Trait
Abdomen abnormality
Clinical name: Abnormal abdomen morphology
A structural abnormality of the abdomen ('belly'), that is, the part of the body between the pelvis and the thorax.
Summary
- Also called
- Abnormality of abdomen structure, Abnormality of abdomen morphology, Abnormality of the abdomen
- Body system
- Abnormality of the digestive system
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Get my Genome Test4 genes linked to Abdomen abnormality
Changes in these genes cause rare conditions in which Abdomen abnormality is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| SPTBN1spectrin beta, non-erythrocytic 1 | Rarely (1–4%) | In 1 condition |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Not recorded | In 1 condition |
| MCOLN1mucolipin TRP cation channel 1 | Not recorded | In 1 condition |
| TMEM67transmembrane protein 67 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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